The role of neurotrophins in neurotransmitter release

被引:102
作者
Tyler, WJ
Perrett, SP
Pozzo-Miller, LD
机构
[1] Univ Alabama, Civitan Int Res Ctr, Dept Psychol, Birmingham, AL 35294 USA
[2] Univ Alabama, Civitan Int Res Ctr, Dept Neurobiol, Birmingham, AL 35294 USA
关键词
BDNF; docked vesicles; fusion pore; hippocampus; mEPSC; Poisson stimulation; quantal release; SNARE proteins; synaptic vesicles; TrkB; voltage-gated Ca2+ channels;
D O I
10.1177/1073858402238511
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The neurotrophins (NTs) have recently been shown to elicit pronounced effects on quantal neurotransmitter release at both central and peripheral nervous system synapses. Due to their activity-dependent release, as well as the subcellular localization of both protein and receptor, NTs are ideally suited to modify the strength of neuronal connections by "fine-tuning" synaptic activity through direct actions at presynaptic terminals. Here, using BDNF as a prototypical example, the authors provide an update of recent evidence demonstrating that NTs enhance quantal neurotransmitter release at synapses through presynaptic mechanisms. The authors further propose that a potential target for NT actions at presynaptic terminals is the mechanism by which terminals retrieve synaptic vesicles after exocytosis. Depending on the temporal demands placed on synapses during high-frequency synaptic transmission, synapses may use two alternative modes of synaptic vesicle retrieval, the conventional slow endosomal recycling or a faster rapid retrieval at the active zone, referred to as "kiss-and-run." By modulating Ca2+ microdomains associated with voltage-gated Ca2+ channels at active zones, NTs may elicit a switch from the slow to the fast mode of endocytosis of vesicles at presynaptic terminals during high-frequency synaptic transmission, allowing more reliable information transfer and neuronal signaling in the central nervous system.
引用
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页码:524 / 531
页数:8
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